34 research outputs found
Sonic Hedgehog Is a Chemoattractant for Midbrain Dopaminergic Axons
Midbrain dopaminergic axons project from the substantia nigra (SN) and the ventral tegmental area (VTA) to rostral target tissues, including the striatum, pallidum, and hypothalamus. The axons from the medially located VTA project primarily to more medial target tissues in the forebrain, whereas the more lateral SN axons project to lateral targets including the dorsolateral striatum. This structural diversity underlies the distinct functions of these pathways. Although a number of guidance cues have been implicated in the formation of the distinct axonal projections of the SN and VTA, the molecular basis of their diversity remains unclear. Here we investigate the molecular basis of structural diversity in mDN axonal projections. We find that Sonic Hedgehog (Shh) is expressed at a choice point in the course of the rostral dopaminergic projections. Furthermore, in midbrain explants, dopaminergic projections are attracted to a Shh source. Finally, in mice in which Shh signaling is inactivated during late neuronal development, the most medial dopaminergic projections are deficient
Extra-Renal Elimination of Uric Acid via Intestinal Efflux Transporter BCRP/ABCG2
Urinary excretion accounts for two-thirds of total elimination of uric acid and the remainder is excreted in feces. However, the mechanism of extra-renal elimination is poorly understood. In the present study, we aimed to clarify the mechanism and the extent of elimination of uric acid through liver and intestine using oxonate-treated rats and Caco-2 cells as a model of human intestinal epithelium. In oxonate-treated rats, significant amounts of externally administered and endogenous uric acid were recovered in the intestinal lumen, while biliary excretion was minimal. Accordingly, direct intestinal secretion was thought to be a substantial contributor to extra-renal elimination of uric acid. Since human efflux transporter BCRP/ABCG2 accepts uric acid as a substrate and genetic polymorphism causing a decrease of BCRP activity is known to be associated with hyperuricemia and gout, the contribution of rBcrp to intestinal secretion was examined. rBcrp was confirmed to transport uric acid in a membrane vesicle study, and intestinal regional differences of expression of rBcrp mRNA were well correlated with uric acid secretory activity into the intestinal lumen. Bcrp1 knockout mice exhibited significantly decreased intestinal secretion and an increased plasma concentration of uric acid. Furthermore, a Bcrp inhibitor, elacridar, caused a decrease of intestinal secretion of uric acid. In Caco-2 cells, uric acid showed a polarized flux from the basolateral to apical side, and this flux was almost abolished in the presence of elacridar. These results demonstrate that BCRP contributes at least in part to the intestinal excretion of uric acid as extra-renal elimination pathway in humans and rats
Modulators of axonal growth and guidance at the brain midline with special reference to glial heparan sulfate proteoglycans
Molecules making waves in axon guidance.
The exquisite complexity of neural connectivity depends upon the precise navigation of axons to their targets in the developing nervous system. How is this achieved? Signals from the environment are assumed to impinge on growth cone receptors and thus steer axons in the right direction, but the molecular details of this process have been largely unknown. Recently, impressive progress has been made in identifying families of molecules that may underlie this process. Candidate diffusible guidance molecules include the netrins and semaphorins, whereas membrane-associated Eph receptors and their ligands are proposed to influence guidance by cellcell contact. Characterization of receptors for some of these molecules now promises the dissection of the signalling pathways that dictate axonal responses to pathfinding cues
Molecules making waves in axon guidance
The exquisite complexity of neural connectivity depends upon the precise navigation of axons to their targets in the developing nervous system. How is this achieved? Signals from the environment are assumed to impinge on growth cone receptors and thus steer axons in the right direction, but the molecular details of this process have been largely unknown. Recently, impressive progress has been made in identifying families of molecules that may underlie this process. Candidate diffusible guidance molecules include the netrins and semaphorins, whereas membrane-associated Eph receptors and their ligands are proposed to influence guidance by cellcell contact. Characterization of receptors for some of these molecules now promises the dissection of the signalling pathways that dictate axonal responses to pathfinding cues
Reticuloendotheliosis type C and primate type D oncoretroviruses are members of the same receptor interference group
The reticuloendotheliosis viruses (REVs), originally isolated from avian species, constitute a group of retroviruses which are more closely related to mammalian retroviruses than to other avian retroviruses. The envelope glycoproteins of members of the REV group display a striking amino acid sequence identity with a group of primate oncoretroviruses which belong to a single receptor interference group and include all of the type D and some type C primate oncoretroviruses. Members of the REV group also have a broad host range which covers most avian cells and some mammalian cells, including those of simian and human origin. In view of this broad host range and the envelope sequence similarities, we investigated the cross-interference pattern between REV and primate virus groups to determine whether they utilized the same receptor. Superinfection experiments using a vector virus containing an Escherichia coli lacZ gene showed that reticuloendotheliosis and simian oncoretroviruses constitute a single receptor interference group on both human and canine cells and indicate that the viruses bind to the same receptor to initiate infection. These results suggest that this receptor binding specificity has been maintained over a wide range of retroviruses and may be responsible for the broad spread of these retroviruses between different orders of vertebrates.</jats:p
